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FDA 510(k)

SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800

K-Number: K023083 · 2003-02-28

ApplicantMettler Electronics Corp.
Decision Date2003-02-28
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800 is the device name listed in this FDA 510(k) record. The listed applicant is Mettler Electronics Corp.. It received FDA 510(k) clearance on 2003-02-28 under 510(k) number K023083. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800?

SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800 is a medical device that received FDA 510(k) clearance on 2003-02-28. The listed applicant is Mettler Electronics Corp.. The 510(k) number is K023083.

When did SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800 receive FDA 510(k) clearance?

SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800 received FDA 510(k) clearance on 2003-02-28, under 510(k) number K023083.

Who is the listed applicant for SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800?

The FDA 510(k) record lists Mettler Electronics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800?

The FDA product code for SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800 is FRN.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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